Resonance fluorescence in transport through quantum dots: noise properties

We study a two-level quantum dot embedded in a phonon bath and irradiated by a time-dependent ac field, and develop a method that allows us to extract simultaneously the full counting statistics of the electronic tunneling and relaxation (by phononic emission) events as well as their correlation. We find that the quantum noise of both the transmitted electrons and the emitted phonons can be controlled by the manipulation of external parameters such as the driving field intensity or the bias voltage.     

An ambipolar peryleneamidine monoimide-fused polythiophene with narrow band gap

A peryleneamidine monoimide-fused terthiophene with a band gap of 1.4 eV has been synthesized. The donor-acceptor system can be electropolymerized to generate a functionalized polythiophene with a band gap of 0.9 eV and with ambipolar characteristics showing high electroactivity in both the p- and the n-doping process. This is the first example of a p-type conjugated polymer in direct conjugation with n-type perylenemonoimide moieties.     

Bioinspired mineralization of inorganics from aqueous media controlled by synthetic polymers

The formation of inorganic structures in nature is commonly controlled by biogenic macromolecules. The understanding of mineralization phenomena and the nucleation and growth mechanisms involved is still a challenge in science but also of great industrial interest. This article focuses on the formation and mineralization of two archetypical inorganic materials: zinc oxide and amorphous calcium carbonate (ACC). Zinc oxide is selected as a model compound to investigate the role that polymers play in mineralization. Most of the effort has been devoted to the investigation of the effects of double-hydrophilic block and graft copolymers. Recent work has demonstrated that latex particles synthesized by miniemulsion polymerization, properly functionalized by various chemical groups, have similar effects to conventional block copolymers and are excellently suited for morphology control of ZnO crystals. Latex particles might serve as analogues of natural proteins in biomineralization. The second example presented, ACC, addresses the issue of whether this amorphous phase is an intermediate in the biomineralization of calcite, vaterite, or aragonite. Conditions under which amorphous calcium carbonate can be obtained as nanometer-sized spheres as a consequence of a liquid-liquid phase segregation are presented. Addition of specific block copolymers allows control of the particle size from the micrometer to the submicrometer length scale. The physical properties of novel materials synthesized from concentrated solution and their potential applications as a filler of polymers are also discussed.     

Commensurability effects for fermionic atoms trapped in 1D optical lattices

Fermionic atoms in two different hyperfine states confined in optical lattices show strong commensurability effects due to the interplay between the atomic density wave ordering and the lattice potential. We show that spatially separated regions of commensurable and incommensurable phases can coexist. The commensurability between the harmonic trap and the lattice sites can be used to control the amplitude of the atomic density waves in the central region of the trap.     

Does Chaplygin gas have salvation?

A mechanism capable to provide a natural solution to two major cosmological problems, i.e. the cosmic acceleration and the coincidence problem, is proposed. A specific brane–bulk energy exchange mechanism produces a total dark pressure, arising when adding all normal to the brane negative pressures in the interior of galactic core black holes. This astrophysically produced negative dark pressure explains cosmic acceleration and why the dark energy today is of the same order to the matter density for a wide range of the involved parameters. An exciting result of the analysis is that the recent rise of the galactic core black hole mass density causes the recent passage from cosmic deceleration to acceleration. Finally, it is worth mentioning that this work corrects a wide spread fallacy among brane cosmologists, i.e. that escaping gravitons result in positive dark pressure.     

Phase equilibrium data and thermodynamic modelling of the system (propane + DMF + methanol) at high pressures

Reported in this work are phase equilibrium data at high pressures for the binary and ternary systems formed by {propane + N,N-dimethylformamide (DMF) + methanol}. Phase equilibrium measurements were performed in a high-pressure, variable-volume view cell, following the static synthetic method for obtaining the experimental bubble and dew points transition data over the temperature range of (363 to 393) K, pressures up to 11.5 MPa and overall mole fraction of the lighter component varying from 0.1 to 0.995. For the systems investigated, vapour–liquid (VLE), liquid–liquid (LLE) and vapour–liquid–liquid (VLLE) phase transitions were visually recorded. Results show that the systems investigated present UCST (upper critical solution temperature) phase transition curves with an UCEP (upper critical end point) at a temperature higher than the propane critical temperature. The experimental data were modelled using the Peng–Robinson equation of state with the Wong–Sandler and the classical quadratic mixing rules, affording a satisfactory representation of the experimental data.     

Quenching enhancement of the singlet excited state of pheophorbide-a by DNA in the presence of the quinone carboquone

Changes in the emission fluorescence intensity of pheophorbide-a (PHEO) in the presence of carboquone (CARBOQ) were used to obtain the association constant, the number of CARBOQ molecules interacting with PHEO, and the fluorescence quantum yield of the complex. Excitation spectra of mixtures of PHEO and CARBOQ in ethanol (EtOH) show an unresolved doublet in the red-most excitation band of PHEO, indicating the formation of a loose ground-state complex. The 1:1 CARBOQ-PHEO complex shows a higher fluorescence quantum yield in EtOH (0.41 ± 0.02) than in buffer solution (0.089 ± 0.002), which is also higher than that of the PHEO monomer (0.28). Quenching of the PHEO fluorescence by DNA nucleosides and double-stranded oligonucleotides was also observed and the bimolecular quenching rate constants were determined. The quenching rate constant increase as the oxidation potential of the DNA nucleoside increases. Larger quenching constants were obtained in the presence of CARBOQ suggesting that CARBOQ enhances DNA photo-oxidation, presumably by inhibiting the back-electron-transfer reaction from the photoreduced PHEO to the oxidized base. Thus, the enhanced DNA-base photosensitized oxidation by PHEO in the presence of CARBOQ may be related to the large extent by which this quinone covalently binds to DNA, as previously reported.     

A comparative photophysical and photochemical study of nitropyrene isomers occurring in the environment

Ground state absorption, first excited-singlet state, and properties of reactive intermediates of mononitropyrene isomers encountered in the atmospheric aerosol have been studied under different conditions that could mimic the environment. The nitro group can present different orientations relative to the pyrene ring depending on its geometric location and could induce differences in the photochemistry of the isomers. The 2-NO(2)Py isomer has the largest red shift and lowest oscillator strength in the UV-visible band associated with the nitro group. The isomers show very low fluorescence yields (10(-3)-10(-4)). Only 1-NO(2)Py and 4-NO(2)Py have phosphorescence emission (Φ(p) ≈ 10(-4)), indicating that the lowest triplet state decays mainly through effective radiationless channels. Laser photolysis produces a low-lying triplet state (τ(T) = 10(-5)-10(-6) s), a long-lived pyrenoxy radical, and a PyNO(2)H radical in solvents in which the triplet can abstract a hydrogen atom. Similar triplet yields were calculated (0.1-0.6) for the isomers, while significant differences in the relative yield of the long-lived species were determined. Differences in the quenching rate constants of the triplet by water and phenols suggest a strong hydrogen-bond interaction with the nitro group in the C-2 position, which provides for radiationless deactivation routes.